# SODIUM SULFATE ANHYDROUS

URL: https://app.greenveil.ai/ingredients/ingredient_dtxsid_dtxsid1021291
Categories: beauty, cleaning, industrial, pharma
Functions: Absorbent, Degradant/impurity, Dye, Filler, Flavouring and nutrient, Flow promoter, Pharmaceutical, Plasticizer, Surfactant (surface active agent), Thickening agent, Viscosity modifier, enzyme coating
Identifier: DTXSID1021291

> SODIUM SULFATE ANHYDROUS is used as absorbent / degradant/impurity. EPA CPDat observed this chemical in 2153 composition records across product categories including Furniture and furnishings, Construction and building materials, Other indirect contact consumer goods. Assessed from 13 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: EPA CPDat observed this chemical in 2153 composition records across product categories including Furniture and furnishings, Construction and building materials, Other indirect contact consumer goods.

## Regulatory status

- US: commercial use observed — EPA CPDat observed this chemical in 2153 composition records across product categories including Furniture and furnishings, Construction and building materials, Other indirect contact consumer goods. EPA CPDat classifies this chemical for functional uses including Viscosity modifier, Absorbent, Filler.
- US: inactive ingredient database — Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Potency: 1.14 %w/v
- US: inactive ingredient database — Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 7 mg
- US: inactive ingredient database — Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Potency: 0.17 %w/w
- US: inactive ingredient database — Route: OPHTHALMIC; Dosage form: SUSPENSION; Potency: 1.2 %w/v
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET; Potency: 96 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, COATED; Potency: NA
- US: inactive ingredient database — Route: RESPIRATORY (INHALATION); Dosage form: SOLUTION; Potency: 0.03 %w/w
- US: marketed drug occurrence — FDA NDC lists this ingredient in 20 active drug products and 20 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as chemical.

_Assessed by Greenveil._